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  5. NDC Package Code: 64725-0798-1 Divalproex Sodium

NDC Package 64725-0798-1 Divalproex Sodium

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
64725-0798-1
Package Description:
100 TABLET, DELAYED RELEASE in 1 BOTTLE
Product Code:
64725-0798
Proprietary Name:
Divalproex Sodium
Usage Information:
This medication is used to treat seizure disorders, certain psychiatric conditions (manic phase of bipolar disorder), and to prevent migraine headaches. It works by restoring the balance of certain natural substances (neurotransmitters) in the brain.
11-Digit NDC Billing Format:
64725079801
NDC to RxNorm Crosswalk:
  • RxCUI: 1099678 - divalproex sodium 250 MG Delayed Release Oral Tablet
  • RxCUI: 1099870 - divalproex sodium 500 MG Delayed Release Oral Tablet
    • Labeler Name:
    Tya Pharmaceuticals
    Sample Package:
    No
    Start Marketing Date:
    07-29-2008
    Listing Expiration Date:
    12-31-2017
    Exclude Flag:
    I
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 64725-0798-1?

    The NDC Packaged Code 64725-0798-1 is assigned to a package of 100 tablet, delayed release in 1 bottle of Divalproex Sodium, labeled by Tya Pharmaceuticals. The product's dosage form is and is administered via form.

    Is NDC 64725-0798 included in the NDC Directory?

    No, Divalproex Sodium with product code 64725-0798 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Tya Pharmaceuticals on July 29, 2008 and its listing in the NDC Directory is set to expire on December 31, 2017 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 64725-0798-1?

    The 11-digit format is 64725079801. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-4-1 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-4-164725-0798-15-4-264725-0798-01